United States · FDA National Drug Code directory
Losartan Potassium
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 68382-137_cfd7f3a9-7719-43af-b0b4-f655824cb19b
- Product NDC
- 68382-137
- Form
- TABLET, FILM COATED
- Composition / generic term
- Losartan Potassium
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20101004
- Source listing expiry
- 20271231
Source-listed ingredients
- LOSARTAN POTASSIUM — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (68382-137-01) · 68382-137-01
- 30 TABLET, FILM COATED in 1 BOTTLE (68382-137-06) · 68382-137-06
- 1000 TABLET, FILM COATED in 1 BOTTLE (68382-137-10) · 68382-137-10
- 90 TABLET, FILM COATED in 1 BOTTLE (68382-137-16) · 68382-137-16
- 10 BLISTER PACK in 1 CARTON (68382-137-77) / 10 TABLET, FILM COATED in 1 BLISTER PACK (68382-137-30) · 68382-137-77
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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